EP3533578B1 - Cleaning agent and method for cleaning resin processing machine - Google Patents
Cleaning agent and method for cleaning resin processing machine Download PDFInfo
- Publication number
- EP3533578B1 EP3533578B1 EP17865536.1A EP17865536A EP3533578B1 EP 3533578 B1 EP3533578 B1 EP 3533578B1 EP 17865536 A EP17865536 A EP 17865536A EP 3533578 B1 EP3533578 B1 EP 3533578B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mass
- purging compound
- parts
- cleaning
- resin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 238000004140 cleaning Methods 0.000 title claims description 63
- 229920005989 resin Polymers 0.000 title claims description 47
- 239000011347 resin Substances 0.000 title claims description 47
- 238000000034 method Methods 0.000 title claims description 32
- 238000012545 processing Methods 0.000 title claims description 25
- 239000012459 cleaning agent Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 113
- 238000010926 purge Methods 0.000 claims description 113
- 229920005992 thermoplastic resin Polymers 0.000 claims description 34
- -1 fatty acid zinc salt Chemical class 0.000 claims description 22
- 239000011256 inorganic filler Substances 0.000 claims description 21
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 21
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 20
- 238000001035 drying Methods 0.000 claims description 20
- 239000011701 zinc Substances 0.000 claims description 20
- 229910052725 zinc Inorganic materials 0.000 claims description 20
- 239000013585 weight reducing agent Substances 0.000 claims description 17
- 239000000194 fatty acid Substances 0.000 claims description 16
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 15
- 229930195729 fatty acid Natural products 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 229920013716 polyethylene resin Polymers 0.000 claims description 4
- 239000000463 material Substances 0.000 description 26
- 239000000203 mixture Substances 0.000 description 24
- 230000000052 comparative effect Effects 0.000 description 12
- 230000008569 process Effects 0.000 description 12
- 239000000155 melt Substances 0.000 description 11
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 10
- 238000004898 kneading Methods 0.000 description 10
- 239000008188 pellet Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 229920001684 low density polyethylene Polymers 0.000 description 9
- 239000004702 low-density polyethylene Substances 0.000 description 9
- 238000000465 moulding Methods 0.000 description 8
- 238000013329 compounding Methods 0.000 description 7
- 238000005187 foaming Methods 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 239000000654 additive Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 229920000092 linear low density polyethylene Polymers 0.000 description 6
- 239000004707 linear low-density polyethylene Substances 0.000 description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- 229920001903 high density polyethylene Polymers 0.000 description 5
- 239000004700 high-density polyethylene Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000012778 molding material Substances 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 150000004996 alkyl benzenes Chemical class 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000007857 degradation product Substances 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000004665 fatty acids Chemical group 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 235000019359 magnesium stearate Nutrition 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229940098697 zinc laurate Drugs 0.000 description 2
- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-UHFFFAOYSA-L 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- MWKGOHCHXBLCSH-UHFFFAOYSA-L [Zn+2].CCCCCCCCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCCCCCCCC([O-])=O Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCCCCCCCC([O-])=O MWKGOHCHXBLCSH-UHFFFAOYSA-L 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 229920003020 cross-linked polyethylene Polymers 0.000 description 1
- 239000004703 cross-linked polyethylene Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000011086 high cleaning Methods 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000007561 laser diffraction method Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229920005653 propylene-ethylene copolymer Polymers 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- YQLFJUAFJLSPPF-CVBJKYQLSA-L zinc (Z)-docos-13-enoate Chemical compound [Zn+2].CCCCCCCC\C=C/CCCCCCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCCCCCC([O-])=O YQLFJUAFJLSPPF-CVBJKYQLSA-L 0.000 description 1
- 229940105125 zinc myristate Drugs 0.000 description 1
- 229940012185 zinc palmitate Drugs 0.000 description 1
- 229940057977 zinc stearate Drugs 0.000 description 1
- LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical compound [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 description 1
- NVKSAUAQUPYOPO-UHFFFAOYSA-L zinc;decanoate Chemical compound [Zn+2].CCCCCCCCCC([O-])=O.CCCCCCCCCC([O-])=O NVKSAUAQUPYOPO-UHFFFAOYSA-L 0.000 description 1
- IJQXGKBNDNQWAT-UHFFFAOYSA-L zinc;docosanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCC([O-])=O IJQXGKBNDNQWAT-UHFFFAOYSA-L 0.000 description 1
- GJAPSKMAVXDBIU-UHFFFAOYSA-L zinc;hexadecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O GJAPSKMAVXDBIU-UHFFFAOYSA-L 0.000 description 1
- PKJOUIVGCFHFTK-UHFFFAOYSA-L zinc;hexanoate Chemical compound [Zn+2].CCCCCC([O-])=O.CCCCCC([O-])=O PKJOUIVGCFHFTK-UHFFFAOYSA-L 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
- GBFLQPIIIRJQLU-UHFFFAOYSA-L zinc;tetradecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCC([O-])=O GBFLQPIIIRJQLU-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C33/00—Moulds or cores; Details thereof or accessories therefor
- B29C33/70—Maintenance
- B29C33/72—Cleaning
- B29C33/722—Compositions for cleaning moulds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/27—Cleaning; Purging; Avoiding contamination
- B29C48/2715—Cleaning; Purging; Avoiding contamination of plasticising units
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
- C08K2003/265—Calcium, strontium or barium carbonate
Definitions
- This disclosure relates to a purging compound that removes degradation products generated from resins or the like, as well as resins and additives such as dyes and pigments processed in a processing machines after the process of the resin completed. More specifically, this disclosure relates to a purging compound that enables cleaning while forming a film and a sheet by a molding machine, without causing film breaking due to the foaming of the purging compound itself during the cleaning. In addition, this disclosure relates to a method of cleaning resin processing machine using such a purging compound.
- Resin processing machines such as an extruder and an injection molding machine are commonly used for processes such as coloring, compounding and molding of resins.
- degradation products for example, thermal decomposition products, carbonized products, char, etc.
- resins and additives such as dyes and pigments processed in a prescribed molding process
- a purging compound is usually obtained by compounding inorganic filler such as calcium carbonate or talc that increases cleaning power, surfactant, lubricant, crosslinked polymer, high-molecular-weight polymer, foaming agent and the other additives with a base polymer.
- inorganic filler such as calcium carbonate or talc that increases cleaning power, surfactant, lubricant, crosslinked polymer, high-molecular-weight polymer, foaming agent and the other additives with a base polymer.
- JP 2006-219568 A (PTL 1) describes a purging compound obtained by compounding polyethylene oxide, alkyl sulfonate, magnesium stearate and other substances with an olefinic thermoplastic resin.
- JP H03-99822 A (PTL 2) describes a purging compound obtained by compounding a ground product of a crosslinked polyethylene film, polyoxyethylene stearyl ether, zinc stearate and other substances with high-density polyethylene.
- JP S60-139411 A (PTL 3) describes a purging compound obtained by compounding calcium carbonate, sodium alkylbenzene sulfonate, sodium stearate, zinc stearate and other substances with linear low-density polyethylene.
- JP 4504699 B (PTL 4) describes a purging compound obtained by mixing sodium bicarbonate with low-density polyethylene containing low-density polyethylene and polypropylene wax.
- JP 4781908 B (PTL 5) describes a purging compound obtained by compounding oleic acid amide, glycerin monostearate and other substances with high-pressure-produced polyethylene
- US5236514 discloses a purging compound comprising a thermoplastic resin, a fatty acid salt, which may be either a sodium or potassium or calcium or zink salt, and an inorganic filler.
- the purging compounds described in PTLs 1 to 3 cannot provide sufficient cleaning effects.
- moisture adsorbed on the polyethylene oxide, alkylbenzene sulfonate, polyoxyethylene stearyl ether and sodium alkylbenzene sulfonate vaporizes, and film breakage due to the foaming of the purging compound itself occurs conspicuously during the cleaning, rendering it difficult to perform cleaning while forming a film.
- the purging compound described in PTL 4 provides recognized cleaning effects, it is difficult to perform cleaning while forming a film with this purging compound because sodium bicarbonate is used as a foaming agent.
- a purging compound that has excellent cleaning performance and enables cleaning while forming a film.
- a method of cleaning a resin processing machine using such a purging compound it is possible to provide a method of cleaning a resin processing machine using such a purging compound.
- the purging compound of the present embodiment contains at least an olefinic thermoplastic resin, fatty acid zinc salt, and inorganic filler and optionally other components.
- the purging compound of the present embodiment is characterized in that the weight reduction rate after drying at 80 °C for 2 hours is 0.2 % or less.
- the purging compound of the present embodiment it is possible to obtain excellent cleaning performance, curb the foaming caused by the water contained in the purging compound during film formation, and clean a resin processing machine while forming a film.
- the purging compound of the present embodiment it is unnecessary to include a special process of preliminarily drying the purging compound or stop the resin processing machine for cleaning, so that continuous cleaning can be performed while performing resin processing such as film formation. In this way, the cleaning efficiency can be further improved.
- thermoplastic resin used in the present embodiment examples include polyethylene resins such as high-density polyethylene, low-density polyethylene and linear low-density polyethylene, polypropylene, polybutene, and propylene-ethylene copolymer.
- polyethylene resins particularly high-density polyethylene, low-density polyethylene and linear low-density polyethylene are preferable.
- the olefinic thermoplastic resin may be used alone or in combination of two or more.
- thermoplastic resins when two or more olefinic thermoplastic resins are used in combination, it is possible to use two or more olefinic thermoplastic resins with different structures in combination, or use two or more olefinic thermoplastic resins with different molecular weights in combination.
- the melt flow rate (MFR) of the olefinic thermoplastic resin is preferably 0.01 g/10 min to 20 g/10 min and more preferably 0.05 g/10 min to 10 g/10 min, from the viewpoints of excellent cleaning power and easy replacement to the subsequent material after cleaning.
- the melt flow rate of the olefinic thermoplastic resin means a melt flow rate measured in accordance with ISO-R1133, where the measurement conditions are a temperature of 190 °C and a load of 2.16 kg.
- thermoplastic resin When a thermoplastic resin is used alone, it is preferable to use one having a melt flow rate within the above ranges. When a plurality of olefinic thermoplastic resins are used, it is preferable to mix those having a melt flow rate within the above ranges, and those having a melt flow rate outside the above ranges and make an adjustment so that the melt flow rate after mixing is within the above ranges.
- the fatty acid moiety of the fatty acid zinc salt preferably has a carbon number of 6 to 28 and more preferably of 10 to 22.
- Specific examples of the fatty acid zinc salt include saturated fatty acid zinc salt such as zinc caproate, zinc caprylate, zinc caprate, zinc laurate, zinc myristate, zinc palmitate, zinc stearate, zinc behenate and zinc montanate, and unsaturated fatty acid zinc salt such as zinc oleate and zinc erucate.
- the fatty acid zinc salt may be used alone or in combination of two or more.
- the content of fatty acid zinc salt is 15 parts by mass to 50 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin, preferably 15 parts by mass to 35 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin, from the viewpoints of excellent cleaning performance, stable continuous film formation cleaning, and stable extrudability of the purging compound composition.
- the content of zinc contained in the purging compound composition is preferably 0.05 parts by mass to 12.0 parts by mass and more preferably 0.1 parts by mass to 10.0 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin.
- the content of zinc contained in the purging compound composition can be measured by an ICP optical emission spectrometer (for example, iCAP 6300 manufactured by Thermo Fisher Scientific K.K.).
- any publicly-known conventional inorganic filler used for resin films and resin sheets may be used as the inorganic filler of the present embodiment without particular limitation.
- Specific examples include metal carbonates such as calcium carbonate, magnesium carbonate and barium carbonate, metal sulfates such as calcium sulfate and barium sulfate, and silicates such as kaolin, clay and diatomaceous earth.
- metal carbonates such as calcium carbonate, magnesium carbonate and barium carbonate
- metal sulfates such as calcium sulfate and barium sulfate
- silicates such as kaolin, clay and diatomaceous earth.
- calcium carbonate and magnesium carbonate are particularly preferable.
- the inorganic filler may be used alone or in combination of two or more.
- the average particle diameter of the inorganic filler is not particularly limited. However, it is preferably 0.1 ⁇ m to 100 ⁇ m, more preferably 0.5 ⁇ m to 50 ⁇ m, and particularly preferably 1 ⁇ m to 30 ⁇ m.
- the average particle diameter of the inorganic filler is within the above ranges, the dispersibility is good, and breakage during film formation or other problems hardly occur. In this way, it is possible to perform continuous film formation cleaning more stably.
- the average particle diameter of the inorganic filler can be determined with a laser diffraction method (using SALD-2000 manufactured by Shimadzu Corporation, for example).
- the content of the inorganic filler is preferably 5 parts by mass to 200 parts by mass, more preferably 10 parts by mass to 150 parts by mass, and particularly preferably 20 parts by mass to 100 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin, from the viewpoints of the effect of physically scraping off the residues remaining inside the processing machine, stable continuous film formation cleaning, and stable extrudability of the purging compound composition.
- the water content of the inorganic filler used for preparing the purging compound is preferably 0.2 mass% or less and particularly preferably 0.1 mass% or less, from the viewpoint of more stable continuous film formation cleaning.
- the purging compound of the present embodiment may contain other resins and various additives according to the cleaning purpose and the performance required for the application, as long as the weight reduction rate of the purging compound composition after drying at 80 °C for 2 hours does not exceed 0.2 %.
- the content of the other components may be, for example, 10 parts by mass or less and preferably 5 parts by mass or less with respect to 100 parts by mass of the olefinic thermoplastic resin.
- the melt flow rate (MFR) of the purging compound of the present embodiment is preferably 0.05 g/10 min to 75 g/10 min and more preferably 0.1 g/10 min to 50 g/10 min, from the viewpoints of excellent cleaning power and easy replacement to the subsequent material after cleaning.
- the melt flow rate of the olefinic thermoplastic resin means a melt flow rate measured in accordance with ISO-R1133, where the measurement conditions are a temperature of 190 °C and a load of 2.16 kg.
- the weight reduction rate after drying at 80 °C for 2 hours is 0.2 % or less, preferably 0.15 % or less, and particularly preferably 0.1 % or less from the viewpoint of stable film formation cleaning.
- the weight reduction rate is preferably 0.01 % or more and more preferably 0.025 % or more.
- the weight reduction rate is more than 0.2 %, a special process of preliminary drying the purging compound is required. If the purging compound in this case is used as it is without the drying process, moisture adsorbed on the purging compound vaporizes, and film breakage due to foaming occurs conspicuously. As a result, it is difficult to perform cleaning while forming a film continuously. In addition, when the weight reduction rate is less than 0.01 %, sufficient cleaning performance may not be obtained.
- the weight reduction rate of the purging compound after drying at 80 °C for 2 hours is determined by leaving the purging compound in an atmosphere with a constant temperature of 25 °C and a constant humidity of 70 % RH for 72 hours, using a constant-temperature drier (for example, DKN 302 manufactured by Yamato Scientific Co., Ltd.) to dry the purging compound at a set temperature of 80 °C under atmospheric pressure for 2 hours, obtaining the masses of the purging compound before and after the drying, and calculating the weight reduction rate based on the masses specifically with the method described in the EXAMPLES section.
- a constant-temperature drier for example, DKN 302 manufactured by Yamato Scientific Co., Ltd.
- examples of the method of setting the weight reduction rate after drying at 80 °C for 2 hours within the aforementioned ranges include a method of adjusting the water content of the inorganic filler and various additives used for preparing the purging compound.
- the purging compound contains highly absorbent additives such as a hydrophilic surfactant or polyethylene oxide
- a special process such as drying the purging compound to remove the moisture just before use is required in order to satisfy the ranges of the weight reduction rate set in the present embodiment, which greatly decreases the working efficiency.
- the method of producing the purging compound of the present embodiment is not particularly limited.
- Examples of a preferred production method include a method of melting and kneading the aforementioned olefinic thermoplastic resin and fatty acid zinc salt, and inorganic filler and other components to be compounded if necessary, with a melt-kneading apparatus, extruding the obtained melt-kneaded product in strand form, and forming the product into granular form.
- the melt-kneading apparatus used here may be a common apparatus used for compounding and melt-kneading various components. Examples thereof include a premixing apparatus such as a tumbler, a ribbon blender and a super mixer, a weight type feeder, a kneader, a single screw extruder or twin screw extruder, a co-kneader, and a Banbury mixer.
- a premixing apparatus such as a tumbler, a ribbon blender and a super mixer, a weight type feeder, a kneader, a single screw extruder or twin screw extruder, a co-kneader, and a Banbury mixer.
- the melt-kneading apparatus is preferably an extruder from the viewpoint of thoroughly kneading the olefinic thermoplastic resin and the inorganic filler.
- the melting and kneading is performed using an extruder, it is desirable to include open deaeration where dissolved air is exhausted through a vent under atmospheric pressure, and, if necessary, depressurization deaeration where dissolved air is exhausted through a vent under reduced pressure.
- the cylinder temperature during the melting and kneading using an extruder is preferably set to 300 °C or lower, more preferably 280 °C or lower, even more preferably 260 °C or lower, and particularly preferably 240 °C or lower.
- the residence time of molten resin in the extruder is as short as possible, and the cylinder temperature is set in consideration of this.
- the purging compound of the present embodiment can be used as it is as a purging compound or used as a mixture with a subsequent material (posterior material) after discharging a preceding material (prior material).
- the purging compound may be previously simply dry-blended with the subsequent material and then used, or may be used while mixing with the subsequent material at a certain ratio using a feeder.
- the purging compound may be previously melt and kneaded with the subsequent material using a resin processing machine and then used.
- the purging compound as a mixture with the subsequent material, from the viewpoint of easy replacement to the subsequent material and stable continuous film formation cleaning.
- the mixing ratio is preferably 100 parts by mass to 900 parts by mass of the subsequent material with respect to 100 parts by mass of the purging compound, more preferably 200 parts by mass to 750 parts by mass of the subsequent material with respect to 100 parts by mass of the purging compound, and even more preferably 300 parts by mass to 600 parts by mass of the subsequent material with respect to 100 parts by mass of the purging compound.
- the content of zinc contained in the resin mixture composed of the purging compound and the subsequent material is preferably 0.02 parts by mass to 5.0 parts by mass and more preferably 0.2 parts by mass to 3.0 parts by mass with respect to 100 parts by mass of the resin mixture, from the viewpoint of maintaining the film formability and high cleaning performance.
- the content of zinc contained in the resin mixture can be measured by an ICP optical emission spectrometer (for example, iCAP 6300 manufactured by Thermo Fisher Scientific K.K.).
- the resin contained in the preceding material is preferably an olefinic resin, and high-density polyethylene, low-density polyethylene and linear low-density polyethylene are particularly preferable among olefinic resins.
- the resin contained in the subsequent material is preferably an olefinic resin, and high-density polyethylene, low-density polyethylene and linear low-density polyethylene are particularly preferable among olefinic resins.
- the purging compound of the present embodiment can be used for any type of resin processing machine without particular limitation.
- the purging compound is particularly suitably used for a sheet and/or a film manufacturing machine, because it curb the foaming caused by heating and enables cleaning while forming a film.
- the method of cleaning a sheet and/or a film manufacturing machine of the present embodiment is characterized in cleaning a sheet and/or a film manufacturing machine with the purging compound of the present embodiment while forming a film continuously.
- the purging compound of the present embodiment may be used in a way as described above.
- a resin composition containing the respective components at the ratios as listed in Tables 1 and 2 was preliminarily mixed for 5 minutes using a tumbler blender, and the obtained mixture was melted and kneaded using a twin screw extruder.
- the melting and kneading was performed using a twin screw extruder (TEM26SS manufactured by Toshiba Machine Co., Ltd.) under the conditions of a cylinder set temperature of 210 °C and a feed rate of 15 kg/hour.
- the melt-kneaded product thus obtained was extruded into strand form, cooled with water, and then cut by a strand cutter to obtain a purging compound in pellet form.
- the melt flow rate (g/10 min) of the obtained purging compound pellets was measured under the conditions of a temperature of 190 °C and a load of 2.16 kg in accordance with ISO-R1133.
- the purging compound pellets were left in an atmosphere with a constant temperature of 25 °C and a constant humidity of 70 % RH for 72 hours, and the mass of the resulting purging compound pellets was measured. Then the above mentioned pretreated pellets were dried using a constant-temperature drier (DKN 302 manufactured by Yamato Scientific Co., Ltd.) at a set temperature of 80 °C under atmospheric pressure for 2 hours, and then the mass was measured again.
- DKN 302 constant-temperature drier manufactured by Yamato Scientific Co., Ltd.
- the weight reduction rate of the obtained purging compound pellets was determined by the following formula. W 1 ⁇ W 2 / W 1 ⁇ 100 % where W1 means the mass before drying of the pellets subjected to the performance evaluation, and W2 means the mass after drying of the pellets subjected to the performance evaluation.
- Table 1 lists the compositions of the purging compounds of Examples 1 to 8, 10 and 11 and Reference Examples 9 and 12 and the evaluation results. *Examples 9 and 12 are Reference Examples Example 1 Example 2 Example 3 Example 4 Example 5 Example 6 Example 7 Example 8 Example 9 Example 10 Example 11 Example 12 Component (A-1) Part by mass 100 100 100 100 100 100 100 100 100 100 Component (A-2) 100 100 Component (B- 1) 20 33 33 33 15 33 33 15 45 15 0.3 Component (B-2) 15 Component (C-1) 80 90 90 90 90 40 40 90 90 90 90 40 40 40 Component (D-1) Component (D-2) Component (E-1) Component (E-2) 3 Zinc content with respect to 100 parts by mass of the polyolefin resin in the purging compound composition Part by mass 2.8 4.6 4.6 4.6 2.1 1.5 4.6 4.6 2.1 6.3 2.0 0.04 MFR [g/10min] 13 21 25 25 9 10 21 21 16 34 11 1 Mixing ratio of purging compound/ subsequent material (in mass) [-] 20/80 20/80 20
- Table 2 lists the compositions of the purging compounds of Comparative Examples 1 to 6 and the evaluation results.
- Comparative Example 1 Comparative Example 2 Comparative Example 3 Comparative Example 4 Comparative Example 5 Comparative Example 6 Component (A-1) Part by mass 100 100 100 100 100 100 Component (A-2) Component (B-1) 15 3 Component (B-2) Component (C-1) 40 80 40 40 40 300 Component (D-1) 15 Component (D-2) 20 Component (E-1) 15 Component (E-2) 15 10 Zinc content with respect to 100 parts by mass of the polyolefin resin in the purging compound composition Part by mass 0.0 0.0 0.0 0.0 2.1 0.42 MFR [g/10min] 2 3 11 10 12 0.8 Mixing ratio of purging compound/ subsequent material (in mass) [-] 20/80 20/80 20/80 20/80 100/0 Zinc content with respect to 100 parts by mass of the resin component containing the subsequent material Part by mass 0.0 0.0 0.0 0.0 0.42 0.42 Cleaning property [-J Poor Poor Good Good Good
- the purging compound of the present disclosure it is possible to provide a purging compound that has excellent cleaning performance and enables cleaning while forming a film.
- the purging compound of the present disclosure has excellent cleaning performance and excellent long-term storability.
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Description
- This disclosure relates to a purging compound that removes degradation products generated from resins or the like, as well as resins and additives such as dyes and pigments processed in a processing machines after the process of the resin completed. More specifically, this disclosure relates to a purging compound that enables cleaning while forming a film and a sheet by a molding machine, without causing film breaking due to the foaming of the purging compound itself during the cleaning. In addition, this disclosure relates to a method of cleaning resin processing machine using such a purging compound.
- Resin processing machines such as an extruder and an injection molding machine are commonly used for processes such as coloring, compounding and molding of resins. With this type of processing machine, degradation products (for example, thermal decomposition products, carbonized products, char, etc.) generated from a resin or the like, as well as resins and additives such as dyes and pigments processed in a prescribed molding process, remain in the processing machine after the process. If these residues are left in the machine, they may, for example, mix with the materials for subsequent processes and cause appearance defects in a resulting product or other problems. Particularly in the case of molding a transparent resin, even only a small amount of mixed residue would cause notable appearance defects in a resulting product, because the residues lower the transparency of the resulting product or make black spots as foreign matters which are visually recognized with ease. Therefore, it is desired to completely remove residues from inside a molding machine.
- In order to remove the residues from inside a processing machine, workers conventionally disassemble and manually clean the processing machine, or perform a so-called replacing process where the inside of the processing machine is cleaned by directly filling the processing machine with a molding material/resin or the like (hereinafter referred to as "subsequent material") to be used subsequently without stopping the processing machine, and discharging the subsequent material together with the residues. In addition, other methods, such as a cleaning method of introducing a purging compound into the processing machine and performing cleaning inside the processing machine, are also being used.
- Among these methods, the method of using a purging compound has been favorably used in recent years because it has excellent cleaning power to remove the residues from inside the processing machine. A purging compound is usually obtained by compounding inorganic filler such as calcium carbonate or talc that increases cleaning power, surfactant, lubricant, crosslinked polymer, high-molecular-weight polymer, foaming agent and the other additives with a base polymer.
- For example,
JP 2006-219568 A -
JP H03-99822 A -
JP S60-139411 A -
JP 4504699 B -
JP 4781908 B -
US5236514 (PTL 6) discloses a purging compound comprising a thermoplastic resin, a fatty acid salt, which may be either a sodium or potassium or calcium or zink salt, and an inorganic filler. -
- PTL 1:
JP 2006-219568 A - PTL 2:
JP H03-99822 A - PTL 3:
JP S60-139411 A - PTL 4:
JP 4504699 B - PTL 5:
JP 4781908 - PTL 6:
US5236514 - However, the purging compounds described in PTLs 1 to 3 cannot provide sufficient cleaning effects. In addition, when the purging compounds are used to clean a molding machine used for forming films such as a resin film and a resin sheet, moisture adsorbed on the polyethylene oxide, alkylbenzene sulfonate, polyoxyethylene stearyl ether and sodium alkylbenzene sulfonate vaporizes, and film breakage due to the foaming of the purging compound itself occurs conspicuously during the cleaning, rendering it difficult to perform cleaning while forming a film.
- It is possible to curb the moisture absorption of the purging compound by storing the purging compound in an environment blocked from the outside air such as a paper bag with an aluminum inner bag. However, once the bag is opened and the purging compound is brought into contact with the outside air, it absorbs moisture immediately. This not only renders it difficult to perform cleaning while forming a film, but also causes problems of poor long-term storability and poor long-term stability.
- If these purging compounds are dried to remove the moisture and then used immediately, it is possible to perform cleaning while forming a film. However, the working efficiency drops significantly because it takes time for the drying process and a special process of providing a dryer is required.
- On the other hand, although the purging compound described in PTL 4 provides recognized cleaning effects, it is difficult to perform cleaning while forming a film with this purging compound because sodium bicarbonate is used as a foaming agent.
- In addition, although it is possible to perform cleaning while forming a film using the purging compound described in PTL 5, the cleaning effects thereof are insufficient and further improvement is required.
- As described above, conventional purging compounds fail to provide sufficient cleaning effects or cause film breakage due to the foaming of the purging compound itself, which renders it difficult to perform cleaning while forming a film. As a result, much time and labor is required for, for example, stopping the process after film formation, performing cleaning only inside the extruder, and then resuming the operation, which significantly reduce the working efficiency.
- It could thus be helpful to provide a purging compound that has excellent cleaning performance and enables cleaning while forming a film. It could also be helpful to provide a method of cleaning a resin processing machine using such a purging compound.
- We made intensive studies to solve the above problems. As a result, we have found that a purging compound where the composition has a specific ratio between olefinic thermoplastic resin and fatty acid zinc salt and the weight reduction rate after drying is not more than a specific value can solve the above problems, and have completed the present disclosure.
- We thus provide the following [1] to [6].
- [1] A purging compound comprising olefinic thermoplastic resin and fatty acid zinc salt, wherein a weight reduction rate after drying at 80 °C for 2 hours is 0.2 % or less, a content of the fatty acid zinc salt is 15 parts by mass to 50 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin, and the purging compound further comprises inorganic filler.
- [2] The purging compound according to [1], wherein a content of zinc is 0.05 parts by mass to 12.0 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin.
- [3] The purging compound according to [1] or [2], wherein the olefinic thermoplastic resin is a polyethylene resin.
- [4] The purging compound according to any one of [1] to [3], wherein a content of the inorganic filler is 5 parts by mass to 200 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin.
- [5] Use of the purging compound according to any one of [1] to [4] in a resin processing machine.
- [6] A method of cleaning a sheet and/or a film manufacturing machine while forming a film continuously by using the purging compound according to any one of [1] to [4].
- According to the present disclosure, it is possible to provide a purging compound that has excellent cleaning performance and enables cleaning while forming a film. In addition, according to the present disclosure, it is possible to provide a method of cleaning a resin processing machine using such a purging compound.
- The following describes an embodiment of the present disclosure in detail. Note that the following embodiment is an example for explaining the present disclosure and that the present disclosure is not limited to the embodiment. Furthermore, various modifications may be made to the present disclosure without departing from the gist thereof.
- The purging compound of the present embodiment contains at least an olefinic thermoplastic resin, fatty acid zinc salt, and inorganic filler and optionally other components.
- The purging compound of the present embodiment is characterized in that the weight reduction rate after drying at 80 °C for 2 hours is 0.2 % or less.
- With the purging compound of the present embodiment, it is possible to obtain excellent cleaning performance, curb the foaming caused by the water contained in the purging compound during film formation, and clean a resin processing machine while forming a film.
- In addition, with the purging compound of the present embodiment, it is possible to curb moisture absorption and thereby obtain excellent long-term storability.
- Furthermore, with the purging compound of the present embodiment, it is unnecessary to include a special process of preliminarily drying the purging compound or stop the resin processing machine for cleaning, so that continuous cleaning can be performed while performing resin processing such as film formation. In this way, the cleaning efficiency can be further improved.
- The following describes the respective components of the purging compound of the present embodiment in detail.
- Specific examples of the olefinic thermoplastic resin used in the present embodiment include polyethylene resins such as high-density polyethylene, low-density polyethylene and linear low-density polyethylene, polypropylene, polybutene, and propylene-ethylene copolymer. Among these, polyethylene resins, particularly high-density polyethylene, low-density polyethylene and linear low-density polyethylene are preferable.
- The olefinic thermoplastic resin may be used alone or in combination of two or more.
- Here, when two or more olefinic thermoplastic resins are used in combination, it is possible to use two or more olefinic thermoplastic resins with different structures in combination, or use two or more olefinic thermoplastic resins with different molecular weights in combination.
- The melt flow rate (MFR) of the olefinic thermoplastic resin is preferably 0.01 g/10 min to 20 g/10 min and more preferably 0.05 g/10 min to 10 g/10 min, from the viewpoints of excellent cleaning power and easy replacement to the subsequent material after cleaning.
- The melt flow rate of the olefinic thermoplastic resin means a melt flow rate measured in accordance with ISO-R1133, where the measurement conditions are a temperature of 190 °C and a load of 2.16 kg.
- When a thermoplastic resin is used alone, it is preferable to use one having a melt flow rate within the above ranges. When a plurality of olefinic thermoplastic resins are used, it is preferable to mix those having a melt flow rate within the above ranges, and those having a melt flow rate outside the above ranges and make an adjustment so that the melt flow rate after mixing is within the above ranges.
- The fatty acid moiety of the fatty acid zinc salt preferably has a carbon number of 6 to 28 and more preferably of 10 to 22. Specific examples of the fatty acid zinc salt include saturated fatty acid zinc salt such as zinc caproate, zinc caprylate, zinc caprate, zinc laurate, zinc myristate, zinc palmitate, zinc stearate, zinc behenate and zinc montanate, and unsaturated fatty acid zinc salt such as zinc oleate and zinc erucate.
- The fatty acid zinc salt may be used alone or in combination of two or more.
- In the present embodiment, the content of fatty acid zinc salt is 15 parts by mass to 50 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin, preferably 15 parts by mass to 35 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin, from the viewpoints of excellent cleaning performance, stable continuous film formation cleaning, and stable extrudability of the purging compound composition.
- In addition, in the present embodiment, the content of zinc contained in the purging compound composition is preferably 0.05 parts by mass to 12.0 parts by mass and more preferably 0.1 parts by mass to 10.0 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin.
- The content of zinc contained in the purging compound composition can be measured by an ICP optical emission spectrometer (for example, iCAP 6300 manufactured by Thermo Fisher Scientific K.K.).
- Any publicly-known conventional inorganic filler used for resin films and resin sheets may be used as the inorganic filler of the present embodiment without particular limitation. Specific examples include metal carbonates such as calcium carbonate, magnesium carbonate and barium carbonate, metal sulfates such as calcium sulfate and barium sulfate, and silicates such as kaolin, clay and diatomaceous earth. Among these, calcium carbonate and magnesium carbonate are particularly preferable.
- The inorganic filler may be used alone or in combination of two or more.
- The average particle diameter of the inorganic filler is not particularly limited. However, it is preferably 0.1 µm to 100 µm, more preferably 0.5 µm to 50 µm, and particularly preferably 1 µm to 30 µm.
- When the average particle diameter of the inorganic filler is within the above ranges, the dispersibility is good, and breakage during film formation or other problems hardly occur. In this way, it is possible to perform continuous film formation cleaning more stably.
- The average particle diameter of the inorganic filler can be determined with a laser diffraction method (using SALD-2000 manufactured by Shimadzu Corporation, for example).
- In the present embodiment, the content of the inorganic filler is preferably 5 parts by mass to 200 parts by mass, more preferably 10 parts by mass to 150 parts by mass, and particularly preferably 20 parts by mass to 100 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin, from the viewpoints of the effect of physically scraping off the residues remaining inside the processing machine, stable continuous film formation cleaning, and stable extrudability of the purging compound composition.
- The water content of the inorganic filler used for preparing the purging compound is preferably 0.2 mass% or less and particularly preferably 0.1 mass% or less, from the viewpoint of more stable continuous film formation cleaning.
- The purging compound of the present embodiment may contain other resins and various additives according to the cleaning purpose and the performance required for the application, as long as the weight reduction rate of the purging compound composition after drying at 80 °C for 2 hours does not exceed 0.2 %.
- The content of the other components may be, for example, 10 parts by mass or less and preferably 5 parts by mass or less with respect to 100 parts by mass of the olefinic thermoplastic resin.
- The following describes the physical properties of the purging compound of the present embodiment.
- The melt flow rate (MFR) of the purging compound of the present embodiment is preferably 0.05 g/10 min to 75 g/10 min and more preferably 0.1 g/10 min to 50 g/10 min, from the viewpoints of excellent cleaning power and easy replacement to the subsequent material after cleaning.
- The melt flow rate of the olefinic thermoplastic resin means a melt flow rate measured in accordance with ISO-R1133, where the measurement conditions are a temperature of 190 °C and a load of 2.16 kg.
- For the purging compound of the present embodiment, the weight reduction rate after drying at 80 °C for 2 hours is 0.2 % or less, preferably 0.15 % or less, and particularly preferably 0.1 % or less from the viewpoint of stable film formation cleaning. In addition, the weight reduction rate is preferably 0.01 % or more and more preferably 0.025 % or more.
- When the weight reduction rate is more than 0.2 %, a special process of preliminary drying the purging compound is required. If the purging compound in this case is used as it is without the drying process, moisture adsorbed on the purging compound vaporizes, and film breakage due to foaming occurs conspicuously. As a result, it is difficult to perform cleaning while forming a film continuously. In addition, when the weight reduction rate is less than 0.01 %, sufficient cleaning performance may not be obtained.
- The weight reduction rate of the purging compound after drying at 80 °C for 2 hours is determined by leaving the purging compound in an atmosphere with a constant temperature of 25 °C and a constant humidity of 70 % RH for 72 hours, using a constant-temperature drier (for example, DKN 302 manufactured by Yamato Scientific Co., Ltd.) to dry the purging compound at a set temperature of 80 °C under atmospheric pressure for 2 hours, obtaining the masses of the purging compound before and after the drying, and calculating the weight reduction rate based on the masses specifically with the method described in the EXAMPLES section.
- In the present embodiment, examples of the method of setting the weight reduction rate after drying at 80 °C for 2 hours within the aforementioned ranges include a method of adjusting the water content of the inorganic filler and various additives used for preparing the purging compound. In a case where the purging compound contains highly absorbent additives such as a hydrophilic surfactant or polyethylene oxide, a special process such as drying the purging compound to remove the moisture just before use is required in order to satisfy the ranges of the weight reduction rate set in the present embodiment, which greatly decreases the working efficiency.
- The method of producing the purging compound of the present embodiment is not particularly limited. Examples of a preferred production method include a method of melting and kneading the aforementioned olefinic thermoplastic resin and fatty acid zinc salt, and inorganic filler and other components to be compounded if necessary, with a melt-kneading apparatus, extruding the obtained melt-kneaded product in strand form, and forming the product into granular form.
- The melt-kneading apparatus used here may be a common apparatus used for compounding and melt-kneading various components. Examples thereof include a premixing apparatus such as a tumbler, a ribbon blender and a super mixer, a weight type feeder, a kneader, a single screw extruder or twin screw extruder, a co-kneader, and a Banbury mixer.
- The melt-kneading apparatus is preferably an extruder from the viewpoint of thoroughly kneading the olefinic thermoplastic resin and the inorganic filler.
- In addition, when the melting and kneading is performed using an extruder, it is desirable to include open deaeration where dissolved air is exhausted through a vent under atmospheric pressure, and, if necessary, depressurization deaeration where dissolved air is exhausted through a vent under reduced pressure.
- The cylinder temperature during the melting and kneading using an extruder is preferably set to 300 °C or lower, more preferably 280 °C or lower, even more preferably 260 °C or lower, and particularly preferably 240 °C or lower.
- It is desirable that the residence time of molten resin in the extruder is as short as possible, and the cylinder temperature is set in consideration of this.
- In the present embodiment, it is more preferable to use a twin screw extruder than other extruders.
- When using a twin screw extruder, it is easy to prevent aggregation of inorganic filler during the melting and kneading of the olefinic resin, fatty acid zinc salt and inorganic filler, and can be easily uniformly dispersed in the olefinic thermoplastic resin. In this way, the extrudability is stabilized, and discharge rate fluctuation of the strand discharged from the extruder and other problems tend to be reduced.
- The purging compound of the present embodiment can be used as it is as a purging compound or used as a mixture with a subsequent material (posterior material) after discharging a preceding material (prior material). For example, the purging compound may be previously simply dry-blended with the subsequent material and then used, or may be used while mixing with the subsequent material at a certain ratio using a feeder. Furthermore, the purging compound may be previously melt and kneaded with the subsequent material using a resin processing machine and then used.
- In the present embodiment, it is preferable to use the purging compound as a mixture with the subsequent material, from the viewpoint of easy replacement to the subsequent material and stable continuous film formation cleaning.
- When the purging compound is used as a mixture with the subsequent material, the mixing ratio is preferably 100 parts by mass to 900 parts by mass of the subsequent material with respect to 100 parts by mass of the purging compound, more preferably 200 parts by mass to 750 parts by mass of the subsequent material with respect to 100 parts by mass of the purging compound, and even more preferably 300 parts by mass to 600 parts by mass of the subsequent material with respect to 100 parts by mass of the purging compound.
- In addition, when the purging compound is used as a mixture with the subsequent material, the content of zinc contained in the resin mixture composed of the purging compound and the subsequent material is preferably 0.02 parts by mass to 5.0 parts by mass and more preferably 0.2 parts by mass to 3.0 parts by mass with respect to 100 parts by mass of the resin mixture, from the viewpoint of maintaining the film formability and high cleaning performance.
- The content of zinc contained in the resin mixture can be measured by an ICP optical emission spectrometer (for example, iCAP 6300 manufactured by Thermo Fisher Scientific K.K.).
- The resin contained in the preceding material is preferably an olefinic resin, and high-density polyethylene, low-density polyethylene and linear low-density polyethylene are particularly preferable among olefinic resins.
- The resin contained in the subsequent material is preferably an olefinic resin, and high-density polyethylene, low-density polyethylene and linear low-density polyethylene are particularly preferable among olefinic resins.
- The purging compound of the present embodiment can be used for any type of resin processing machine without particular limitation. However, the purging compound is particularly suitably used for a sheet and/or a film manufacturing machine, because it curb the foaming caused by heating and enables cleaning while forming a film.
- The method of cleaning a sheet and/or a film manufacturing machine of the present embodiment is characterized in cleaning a sheet and/or a film manufacturing machine with the purging compound of the present embodiment while forming a film continuously.
- The purging compound of the present embodiment may be used in a way as described above.
- The following describes the present disclosure in more detail with reference to Examples and Comparative Examples, yet the present disclosure is not limited thereto.
- The respective components used in Examples or Comparative Examples are as follows.
-
- (A-1) low-density polyethylene (MFR: 2 g/10 min)
- (A-2) linear low-density polyethylene (MFR: 0.8 g/10 min)
-
- (B-1) zinc laurate (zinc content: 14.0 mass%)
- (B-2) zinc stearate (zinc content: 10.3 mass%)
- (C-1) calcium carbonate (average particle diameter: 7 µm)
-
- (D-1) calcium stearate
- (D-2) magnesium stearate
-
- (E-1) sodium alkylbenzene sulfonate (product name: NEOPELEX G-15, manufactured by Kao Corporation)
- (E-2) polyethylene glycol (number average molecular weight: 11,000)
- A resin composition containing the respective components at the ratios as listed in Tables 1 and 2 was preliminarily mixed for 5 minutes using a tumbler blender, and the obtained mixture was melted and kneaded using a twin screw extruder. The melting and kneading was performed using a twin screw extruder (TEM26SS manufactured by Toshiba Machine Co., Ltd.) under the conditions of a cylinder set temperature of 210 °C and a feed rate of 15 kg/hour. The melt-kneaded product thus obtained was extruded into strand form, cooled with water, and then cut by a strand cutter to obtain a purging compound in pellet form.
- The method of evaluating the purging compounds in Examples or Comparative Examples is as follows.
- Sampling was performed in the obtained purging compound pellets, and the sample was measured by an ICP optical emission spectrometer (iCAP 6300 manufactured by Thermo Fisher Scientific K.K.) to calculate the content of zinc contained in the purging compound. The zinc content was expressed in part by mass with respect to 100 parts by mass of the olefinic thermoplastic resin.
- The melt flow rate (g/10 min) of the obtained purging compound pellets was measured under the conditions of a temperature of 190 °C and a load of 2.16 kg in accordance with ISO-R1133.
- The purging compound pellets were left in an atmosphere with a constant temperature of 25 °C and a constant humidity of 70 % RH for 72 hours, and the mass of the resulting purging compound pellets was measured. Then the above mentioned pretreated pellets were dried using a constant-temperature drier (DKN 302 manufactured by Yamato Scientific Co., Ltd.) at a set temperature of 80 °C under atmospheric pressure for 2 hours, and then the mass was measured again.
-
- First, 150 g of a green-colored molding material of low-density polyethylene, which was a preceding resin, was put into a sheet molding machine (with a width of 50 mm and a screw diameter of 19 mm) at a cylinder temperature of 180 °C to form a sheet.
- Subsequently, 200 g of a resin mixture obtained by mixing the aforementioned purging compound with low-density polyethylene, which was a subsequent resin, at the ratio listed in Tables 1 and 2 was charged into the sheet molding machine to clean the inside of the machine.
- After the cleaning finished, the cleaning and film forming properties of the purging compound pellets obtained in Examples and Comparative Examples were evaluated based on the states of the processing machine and the subsequent resin according to the following evaluation criteria.
- Excellent: the green-colored molding material was completely removed.
- Good: the green-colored molding material was almost removed.
- Poor: the green-colored molding material remained.
-
- Good: the sheet itself did not foam and was able to be wound.
- Fair: although foaming was observed in the sheet, the sheet was still able to be wound.
- Poor: the sheet itself foamed conspicuously and was unable to be wound.
- Sampling was performed in the resin mixture composed of the purging compound and the subsequent resin prepared in the aforementioned [cleaning property and film forming property] evaluation, and the sample was measured by an ICP optical emission spectrometer (iCAP 6300 manufactured by Thermo Fisher Scientific K.K.) to calculate the zinc content in the resin mixture. The zinc content was expressed in part by mass with respect to 100 parts by mass of the resin component of the entire mixture.
- Table 1 lists the compositions of the purging compounds of Examples 1 to 8, 10 and 11 and Reference Examples 9 and 12 and the evaluation results.
*Examples 9 and 12 are Reference Examples Example 1 Example 2 Example 3 Example 4 Example 5 Example 6 Example 7 Example 8 Example 9 Example 10 Example 11 Example 12 Component (A-1) Part by mass 100 100 100 100 100 100 100 100 100 100 Component (A-2) 100 100 Component (B- 1) 20 33 33 33 15 33 33 15 45 15 0.3 Component (B-2) 15 Component (C-1) 80 90 90 90 40 40 90 90 90 40 40 Component (D-1) Component (D-2) Component (E-1) Component (E-2) 3 Zinc content with respect to 100 parts by mass of the polyolefin resin in the purging compound composition Part by mass 2.8 4.6 4.6 4.6 2.1 1.5 4.6 4.6 2.1 6.3 2.0 0.04 MFR [g/10min] 13 21 25 25 9 10 21 21 16 34 11 1 Mixing ratio of purging compound/ subsequent material (in mass) [-] 20/80 20/80 20/80 40/60 20/80 20/80 5/95 60/40 20/80 20/80 20/80 100/0 Zinc content with respect to 100 parts by mass of the resin component containing the subsequent material Part by mass 0.57 0.93 0.93 1.87 0.42 0.31 0.23 2.80 0.42 1.27 0.42 0.04 Cleaning property [-] Good Excellent Excellent Excellent Good Good Good Good Excellent Excellent Good Fair Film forming property [-] Good Good Good Good Good Good Good Fair Good Good Fair Good Weight reduction rate after drying at 80 °C for 2 hours [%] [%] 0.08 0.08 0.07 0.07 0.03 0.07 0.08 0.08 0.05 0.09 0.2 0.02 - Table 2 lists the compositions of the purging compounds of Comparative Examples 1 to 6 and the evaluation results.
Comparative Example 1 Comparative Example 2 Comparative Example 3 Comparative Example 4 Comparative Example 5 Comparative Example 6 Component (A-1) Part by mass 100 100 100 100 100 100 Component (A-2) Component (B-1) 15 3 Component (B-2) Component (C-1) 40 80 40 40 40 300 Component (D-1) 15 Component (D-2) 20 Component (E-1) 15 Component (E-2) 15 10 Zinc content with respect to 100 parts by mass of the polyolefin resin in the purging compound composition Part by mass 0.0 0.0 0.0 0.0 2.1 0.42 MFR [g/10min] 2 3 11 10 12 0.8 Mixing ratio of purging compound/ subsequent material (in mass) [-] 20/80 20/80 20/80 20/80 20/80 100/0 Zinc content with respect to 100 parts by mass of the resin component containing the subsequent material Part by mass 0.0 0.0 0.0 0.0 0.42 0.42 Cleaning property [-J Poor Poor Good Good Good Good Film forming property [-] Good Good Poor Poor Poor Poor Weight reduction rate after drying at 80 °C for 2 hours [%] 0.1 0.05 0.55 0.45 0.42 0.3 - According to the present disclosure, it is possible to provide a purging compound that has excellent cleaning performance and enables cleaning while forming a film. The purging compound of the present disclosure has excellent cleaning performance and excellent long-term storability. In addition, it is unnecessary to perform a special process of preliminarily drying the purging compound or stop the cleaning of a sheet and/or a film manufacturing machine, so that cleaning can be performed continuously while forming a film and the cleaning efficiency can be further improved. Therefore, the purging compound of the present disclosure is highly valued in industry.
Claims (6)
- A purging compound comprising olefinic thermoplastic resin and fatty acid zinc salt, wherein a weight reduction rate after drying at 80 °C for 2 hours is 0.2 % or less,
a content of the fatty acid zinc salt is 15 parts by mass to 50 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin, and
the purging compound further comprises inorganic filler. - The purging compound according to claim 1, wherein a content of zinc is 0.05 parts by mass to 12.0 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin.
- The purging compound according to claim 1 or 2, wherein the olefinic thermoplastic resin is a polyethylene resin.
- The purging compound according to any one of claims 1 to 3, wherein a content of the inorganic filler is 5 parts by mass to 200 parts by mass with respect to 100 parts by mass of the olefinic thermoplastic resin.
- Use of the purging compound according to any one of claims 1 to 4 in a resin processing machine.
- A method of cleaning a sheet and/or a film manufacturing machine while forming a film continuously by using the purging compound according to any one of claims 1 to 4.
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JP2016210936 | 2016-10-27 | ||
PCT/JP2017/036523 WO2018079237A1 (en) | 2016-10-27 | 2017-10-06 | Cleaning agent and method for cleaning resin processing machine |
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JP (1) | JP6710774B2 (en) |
CN (1) | CN109689326B (en) |
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CN112236281B (en) * | 2018-05-16 | 2023-02-17 | 俾提提公共有限公司 | Purging compound for cleaning plastic molding machines and mixers |
JP7036478B1 (en) * | 2020-11-27 | 2022-03-15 | 林化成株式会社 | Detergent for molding machines |
Family Cites Families (13)
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CA857357A (en) * | 1969-04-01 | 1970-12-01 | Chemcell Limited | Addition of zinc stearate to polypropylene prior to extrusion |
JPS60139411A (en) * | 1983-12-27 | 1985-07-24 | Wako Kasei Kogyo Kk | Cylinder cleaning agent for thermoplastic synthetic resin molding machine |
JPH0399822A (en) | 1989-09-14 | 1991-04-25 | Tonen Chem Corp | Purging agent of extruder |
US5236514A (en) * | 1990-06-06 | 1993-08-17 | Union Carbide Chemicals & Plastics Technology Corporation | Purging composition for cleaning thermoplastic processing equipment |
JP3109627B2 (en) * | 1992-09-11 | 2000-11-20 | チッソ株式会社 | Resin composition for cleaning in extruder for inflation film |
KR950018227A (en) * | 1993-12-27 | 1995-07-22 | 사토 아키오 | Polypropylene Resin Composition |
JP3988057B2 (en) * | 1996-01-29 | 2007-10-10 | ダイセル化学工業株式会社 | Cleaning resin composition |
JP2000159928A (en) * | 1998-11-25 | 2000-06-13 | Chisso Corp | Thermoplastic resin composition for cleaning |
JP4504699B2 (en) | 2004-02-18 | 2010-07-14 | 旭化成ケミカルズ株式会社 | Cleaning agent for molding machine |
JP2006219568A (en) | 2005-02-09 | 2006-08-24 | Nippon A & L Kk | Resin composition for cleaning inflation extrusion molding machine and using method thereof |
JP2007021765A (en) * | 2005-07-12 | 2007-02-01 | Nippon A & L Kk | Washing resin composition for molding machine and washing method |
JP4781908B2 (en) | 2006-05-24 | 2011-09-28 | 日本ユニカー株式会社 | Resin composition for cleaning plastic molding machines |
EP2922908A2 (en) * | 2012-11-20 | 2015-09-30 | The Procter & Gamble Company | Polymer-soap compositions and methods of making and using the same |
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2017
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CN109689326B (en) | 2021-08-24 |
CN109689326A (en) | 2019-04-26 |
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JPWO2018079237A1 (en) | 2019-04-25 |
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